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rs397516469

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397516469(C;T)
Make rs397516469(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position201363391
GeneTNNT2
is asnp
is mentioned by
dbSNPrs397516469
ebirs397516469
HLIrs397516469
Exacrs397516469
Varsomers397516469
Maprs397516469
PheGenIrs397516469
hapmaprs397516469
1000 genomesrs397516469
hgdprs397516469
ensemblrs397516469
gopubmedrs397516469
geneviewrs397516469
scholarrs397516469
googlers397516469
pharmgkbrs397516469
gwascentralrs397516469
openSNPrs397516469
23andMers397516469
23andMe allrs397516469
SNP Nexus

SNPshotrs397516469
SNPdbers397516469
MSV3drs397516469
GWAS Ctlgrs397516469
Max Magnitude0
ClinVar
Risk rs397516469(T;T)
Alt rs397516469(T;T)
Reference rs397516469(C;C)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy
Variation info
Gene TNNT2
CLNDBN Primary dilated cardiomyopathy
Reversed 1
HGVS NC_000001.10:g.201332519G>A
CLNSRC ClinVar
CLNACC RCV000036594.2,